S-EB-S block copolymer/oil aqueous dispersion and its use in forming articles

ABSTRACT

An aqueous dispersion has particles dispersed in a continuous dispersion medium. The particles, preferably no more than about 2 micrometers in size, are formed of a mixture of styrene-ethylene/butylene-styrene (S-EB-S) block copolymer having end blocks each with a weight average molecular weight of more than about 15,000 Daltons and an oil such as a mineral oil. The dispersion medium is a mixture of water and a surfactant. Articles are prepared by dipping a form into the dispersion and withdrawing the form to leave a film of the dispersion on the form. The water is evaporated from the film, leaving a coherent extensible film on the form.

BACKGROUND OF THE INVENTION

This invention relates to aqueous dispersions of S-EB-S block copolymerand the use of such aqueous dispersions in forming articles, preferablyby dip forming.

Thin-walled, extensible articles such as gloves, condoms, and otherproducts have long been made from natural rubber. In normal production,such articles are formed from natural rubber latex, a naturallyoccurring emulsion of rubber and water, with added stabilizing agentsand vulcanizing chemicals. A form of the appropriate shape, previouslycoated with a coagulating solution in some cases, is dipped into thelatex mixture once or several times to build up a layer of the desiredthickness. The water is allowed to evaporate, leaving a solid rubberfilm. The film must be vulcanized to provide adequate mechanical andphysical properties.

Natural rubber has many advantages in these applications, being strongand highly elastic and having good "tactility" or feeling to the user.Natural rubber has several shortcomings, such as susceptibility to"pinholes" therethrough, rapid attack by ozone which causes scissioncracking, and oxidative attack during storage which causes cracking anddestroys the physical integrity of the product. Natural rubber is alsonot hypoallergenic due to the residual surfactants, vulcanizing agents,stabilizing agents, antioxidants, and/or protein materials in therubber. Persons who are particularly susceptible to irritation orsensitization, or use the rubber products for extended periods of timemay experience allergic reactions.

Various types of synthetic elastomeric polymer products have beendeveloped for use in thin articles produced by dip forming. Syntheticrubber compositions can be dissolved in solvents to form a truesolution, so that pinholes are much less likely to be present. Manyavailable synthetic rubber compositions have various other shortcomings,including unacceptable tactility. While each may meet some of therequirements, most do not have the required combination of strength,tactility, resistance to environmental damage, and hypoallergenicityrequired for many products such as examination and surgical gloves,condoms, and other medical products that are to come into contact withthe human body.

An important advance in the art of synthetic elastomeric polymerproducts is described in U.S. Pat. Nos. 5,112,900 and 5,407,715. Thesepatents disclose the preparation of specificstyrene-ethylene/butylene-styrene (S-EB-S) block copolymer solutions andtheir use in the dip forming of articles. The resulting articles haveexcellent elastomeric properties for use in gloves, condoms, and otherproducts. They exhibit low incidence of pinholes, good resistance toenvironmental damage such as oxidation and ozonation, andhypoallergenicity.

There is, however, always a need to further improve themanufacturability of articles made of such formulations and the processeconomics. The present invention fulfills this need, and furtherprovides related advantages.

SUMMARY OF THE INVENTION

The present invention provides an S-EB-S aqueous dispersion and anapproach for utilizing that aqueous dispersion in the preparation ofthin elastomeric articles. The articles have the desirablecharacteristics of comparable articles made from S-EB-S solutions,including excellent elastomeric properties, low incidence of pinholes,good resistance to environmental damage such as oxidation and ozonation,and hypoallergenicity. Additionally, the dip-forming manufacturingoperation functions at greater rates for improved process economics, ascompared with the prior approach. Thicker layers or articles may be madein each dip-forming step. The manufacturing operation is also safer dueto the absence of toxic solvents during the dip-forming process.

In accordance with the invention, an aqueous dispersion comprises adispersion medium comprising a mixture of water and a surfactant, and aplurality of particles dispersed in the dispersion medium. Each particlecomprises a mixture of an S-EB-S (styrene-ethylene/butylene-styrene)block copolymer, and an oil such as a mineral oil. Most preferably, theparticles are of an average size of no greater than about 2 micrometers.The S-EB-S block copolymer, which may be formed of molecules ofsubstantially the same molecular weight or mixtures of two or moremolecular weights, preferably have end block weight average molecularweights of each of the end blocks of more than about 15,000 Daltons.

The aqueous dispersion may be used in a dip-forming method formanufacturing thin-walled articles. In accordance with this aspect ofthe invention, a method for the preparation of an elastomeric articlecomprises the steps of furnishing an aqueous dispersion of the typedescribed, dipping a form into the aqueous dispersion and withdrawingthe form from the aqueous dispersion, leaving a film of the dispersionon the form, and evaporating the water from the dispersion on the formand fusing the remaining material, leaving a coherent extensible film onthe form. The aqueous dispersion used in the dip-forming method issubstantially free of non-aqueous solvents, but trace amounts that maybe present are not detrimental in the dip-forming process, and may, insome cases, be beneficial in forming a coherent film.

The aqueous dispersion may be used in conjunction with other processingtechniques. For example, the aqueous dispersion may be used in thecoagulant dipping process that is utilized for natural latex rubbercompounds. It also may be used, for example, in spray coating or slushmolding operations.

The resulting article has the desirable features associated with theS-EB-S block copolymer as described U.S. Pat. Nos. 5,112,900 and5,407,715, whose disclosures are incorporated by reference.Additionally, the articles may be made much more quickly than possiblewith the solution-based approach described in these patents. In themanufacturing operation, the dispersion is normally made at one locationwhich has apparatus for disposing of the potentially toxic solventvapors evolved during preparation of the dispersion. The dip-formingoperation may be performed elsewhere. Because there is no potentiallytoxic solvent evolved in the dip-forming operation, there is little riskof injury to workers on the dip-forming and drying line.

Other features and advantages of the present invention will be apparentfrom the following more detailed description of the preferredembodiment, taken in conjunction with the accompanying drawings, whichillustrate, by way of example, the principles of the invention. Thescope of the invention is not, however, limited to this preferredembodiment.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a block flow diagram of a preferred approach for practicingthe invention;

FIG. 2A is a schematic microstructural view of an(S-EB-S/oil)-in-(water/surfactant) aqueous dispersion;

FIG. 2B is a schematic microstructural view of a(water/surfactant)-in-(S-EB-S/oil) aqueous dispersion;

FIG. 3 is a perspective view of a glove form; and

FIG. 4 is a perspective view of a male condom form.

DETAILED DESCRIPTION OF THE INVENTION

FIG. 1 is a block flow diagram depicting a preferred approach forpreparing an aqueous dispersion in accordance with the invention, andthen for using that aqueous dispersion to prepare an article by dipforming.

A styrene-ethylene/butylene-styrene (S-EB-S) block copolymer isprovided, numeral 20. The S-EB-S block copolymer is formed from anethylene-butylene copolymer central block and polystyrene end blocks.The polystyrene end blocks each have a weight average molecular weightof at least about 15,000 Daltons, and, more preferably, at least fromabout 20,000 to about 25,000 Daltons. Because there is a relativelylarge amount of oil in the dip-forming solution, it is beneficial thatthe S-EB-S block copolymer have a high end block polystyrene content,achieved with these end block molecular weights. If the weight averagemolecular weights of each of the end blocks are less than about 15,000,articles can be formed by dip forming, but their strengths are reducedand unacceptably low for some applications. The polystyrene end blockstypically constitute about 25-35 percent by weight of the totalmolecule. The total molecular weight of the copolymer is typically fromabout 50,000 to about 300,000 Daltons.

The S-EB-S block copolymer may optionally have end-block compatibleresins added to the polystyrene end blocks. The added end-blockcompatible resin increases the glass transition temperature (T_(g)) ofthe S-EB-S block copolymer. The increased T_(g) allows the finalproducts to be used at higher temperatures than otherwise possible, asthe product tends to become somewhat sticky at and above T_(g). Anexample of such an end-block compatible resin is poly alpha methylstyrene.

The S-EB-S block copolymer is to be distinguished from other blockcopolymers that have sometimes been used in synthetic rubbercompositions, such as styrene-isoprene-styrene (S-I-S) andstyrene-polybutydiene-styrene (S-B-S) block copolymers. It has beenknown to make thin rubberlike articles from S-I-S and S-B-S blockcopolymers, see for example, U.S. Pat. No. 3,933,723. The use of theseS-I-S and S-B-S block copolymers eliminates the need for vulcanizationof the articles, but the articles are subject to oxidation and ozonedamage.

The use of an S-EB-S block copolymer, as distinct from other types, iscritical to the success of the present invention, for two reasons.First, elastomers based upon the S-EB-S block elastomeric triblockcopolymers are resistant to attack by ozone, or by oxidative conditions,while S-I-S and S-B-S elastomers suffer from rapid cracking, whenexposed to ozone, and cracking or hardening under oxidative conditions.Both of the latter copolymers are thus subject to failure even whenprotected by specific additives such as antiozonants or antioxidantswhich are deleterious in medical and other applications. The use of suchspecial additives is undesirable, as they may cause allergic reactionsin some persons. The present elastomeric composition is hypoallergenicand may be contacted with the skin of the user for extended periods oftime. Additionally, in spite of the special additives, scission crackingcan lead to premature failure by ozone cracking of the articles madefrom S-I-S and S-B-S compositions, particularly when the articles arestored in a folded condition and then stretched before and during use.

Second, the mechanical properties of the S-EB-S triblock copolymers maybe selected to provide the desirable combination of tensile strength,elasticity, and tactility that is required in some applications. S-EB-Selastomeric triblock copolymers have higher tensile strength, lowerelastic elongation, and higher stress at 50-500 percent elongation thanthe S-I-S and S-B-S triblock elastomers.

The structure, properties, and some applications of some S-EB-Selastomers have been disclosed in U.S. Pat. Nos. 3,485,787; 3,830,767;4,006,116; 4,039,629; 4,041,103; 4,386,179; 4,481,323; 4,511,354; and4,613,640, whose disclosures are incorporated by reference.

The S-EB-S block copolymers are available commercially in a range ofsolution viscosity/copolymer concentration values. The solutionviscosity/copolymer concentration value is determined by measuring theviscosity of a copolymer that has been previously dissolved in a solventat a specified level. The solution viscosity/copolymer concentrationvalue is a conventional approach for uniquely defining the nature of ablock copolymer whose central and end block content has been specifiedby type and relative amount. For example, an S-EB-S block copolymer isuniquely specified by the stated composition of polystyrene end blocksand poly-(ethylene-butylene) central blocks, the relative amount of endblocks and central blocks, and the solution viscosity/copolymerconcentration. Thus, a block copolymer is uniquely defined by statingthat it is of the S-EB-S type, that the percentage of polystyrene endblocks is, for example, 28 percent by weight of the total copolymer, andthat the Brookfield Viscosity of a 20 weight percent solution in tolueneat 77° F. is 1500 CPS.

The commercially available S-EB-S block copolymers are manufactured in aprecise manner so that each of the commercially available materials isclosely controlled to meet such standards. Shell Kraton 1650 is anS-EB-S block copolymer having a styrene/central block ratio of 28/72 anda Brookfield Viscosity in toluene solution (20 percent concentration byweight) at 77° F. of 1500. Shell Kraton 1651 is an S-EB-S blockcopolymer having a styrene/central block ratio of 33/67 and a BrookfieldViscosity in toluene solution (20 percent concentration by weight) at77° F. of 2000. Shell Kraton 1652 is an S-EB-S block copolymer having astyrene/central block ratio of 29/71 and a Brookfield Viscosity intoluene solution (20 percent concentration by weight) at 77° F. of 550.

The S-EB-S block copolymer may comprise molecules with substantially thesame molecular weight. It may also comprise mixtures of molecules withtwo or more different molecular weights. The molecular weights and/ormixtures of molecular weights are selected to contribute to achievingdesired mechanical properties in the final product. For example, in onepreferred embodiment, mixtures of S-EB-S molecules as disclosed in U.S.Pat. Nos. 5,112,900 and 5,407,715 are utilized in order to achieve therequired mechanical properties to meet ASTM specifications.

An oil (also sometimes termed a "plasticizer") is provided, numeral 22.The oil is preferably a mineral oil, which is a refined petroleumnapthenic hydrocarbon oil described in Entries 6971 and 6972 of theMerck Index, Eighth Edition. The preferred mineral oil has a specificgravity of 0.87 at 77° F., a viscosity of 170 centistokes at 77° F., anda Hirschler molecular weight of 492. The selected oil should not swellor solubilize the polystyrene end segments.

The S-EB-S block copolymer is furnished by the manufacturer as a solid.To form a mixture from which a suitable dispersion may be prepared, asolvent (toluene or cyclohexane in the preferred approach) is provided,numeral 24. The S-EB-S block copolymers and the mineral oil plasticizerare mixed together and dissolved in a mutual solvent, preferably tolueneor cyclohexane, numeral 26.

A dispersion medium is prepared from water, numeral 28, and asurfactant, numeral 30. The surfactant may be an anionic or cationicform, or mixture of ionic and nonionic types. Suitable surfactants aredisclosed in U.S. Pat. Nos. 3,360,599; 3,305,917; and 5,120,765, whosedisclosures are incorporated by reference. The preferred surfactant isan anionic surfactant. Cationic surfactants are operable but lesspreferred, because cationic surfactants may be allergenic but mostanionic surfactants are hypo-allergenic. Although most of the surfactantand its residues are leached out and removed during the manufacturingoperation, small amounts may remain and may cause an allergic reactionin the product user, if the surfactant is not hypo-allergenic. Thesurfactant 30 is mixed with the water, numeral 32, in an amount of fromabout 1 to about 5 percent by volume. The surfactant 30 may also beproduced in situ by adding and reacting surfactant-forming chemicals.For example, oleic acid added to the oil phase (the S-EB-S solution) andpotassium hydroxide added to the water phase react to form thesurfactant potassium oleate upon mixing.

Optionally, modifying additives such as thickeners, defoamers, orbuffers may also be supplied and added to the aqueous dispersion medium,numeral 31.

The mixture 26 of S-EB-S, oil, and solvent is mixed together with themixture 32 of water and surfactant, numeral 34. The mixing 34 isperformed under high-speed, high-shear-rate conditions using a mixerdesigned to produce dispersions. A preferred mixer is a rotor/statormixer such as an X-series mixer available from Charles Ross & Co or aMicrofluidizer M210 available from Microfluidics Co. Several high-shearmixing passes may be required to obtain the desired particle size.

Equivalently to the procedure discussed in relation to steps 20-34, thecomponents may be mixed and the dispersion formed in other orders and byother paths. For example, in another approach the S-EB-S blockcopolymer, the solvent, and some of the water are mixed together underhigh-shear conditions to form a first dispersion, and the oil andadditional water are mixed together under high-shear conditions to forma second dispersion. Modifiers may be dispersed into either of thedispersions. The first dispersion and the second dispersion arethereafter mixed together to form a third dispersion. Yet othervariations may also be used.

After dispersing step 34, the solvent (toluene or cyclohexane in thepreferred approach) is removed from the dispersion, numeral 36, a stepoften termed "stripping". Stripping may be accomplished by any operableapproach, with vacuum stripping, heat/vacuum stripping, or steamstripping preferred. The solvent has the highest vapor pressure of anyof the components of the dispersion, and it is therefore vaporized anddrawn out of the dispersion. Additional water may also be added in step36, or water may be removed by heating or other approach in aconcentration step 37. Optionally, a biocide may be added in step 37 aswell.

FIGS. 2A and 2B illustrate two possible types of dispersions produced bythe present approach of steps 20-36, an(S-EB-S/oil)-in-(water/surfactant) aqueous dispersion (FIG. 2A) and a(water/surfactant)-in-(S-EB-S/oil) aqueous dispersion (FIG. 2B). Thetype of dispersion produced is responsive to the relative amounts of themixture 26 and the mixture 32 that remain after the stripping step 36,as well as the type and amount of the surfactant (which alters thesurface energies of the phases). If a relatively small amount of(S-EB-S/oil)-solvent mixture is present, as compared with the amount of(water/surfactant) mixture, the dispersion has a structure of discretedroplets 50 of (S-EB-S/oil)-solvent mixture in a continuous(water/surfactant) phase 52, as depicted in FIG. 2A. In the dispersionof FIG. 2A, the (S-EB-S/oil) particles 50 are generally spherical withan average size of no more than about 2 micrometers. If the particlesare significantly larger, they have a tendency to separate and thedispersion is not stable. If a relatively large amount of(S-EB-S/oil)-solvent mixture is present, as compared with the amount of(water/surfactant) mixture, the dispersion has a structure of discretedroplets 54 of (water/surfactant) phase in a continuous(S-EB-S/oil)-solvent mixture 56, as depicted in FIG. 2B. (Thewater/surfactant phase is termed the "dispersion medium" herein, whetherit forms the continuous phase or, during intermediate stages of theprocessing, the dispersed phase.)

The (S-EB-S/oil)-in-(water/surfactant) aqueous dispersion of FIG. 2A isuseful for dip-forming operations. The(water/surfactant)-in-(S-EB-S/oil/solvent) aqueous dispersion (FIG. 2B)is a transient system present only during the preparation of the aqueousdispersion used in dip-forming operations.

Both types of dispersions of FIGS. 2A and 2B may be present at differenttimes (but not coexisting) during the course of the preparation of thedispersion in steps 20-34. For example, in a preferredinverse-dispersion approach as described in U.S. Pat. Nos. 2,872,427 and3,867,321, and Canadian Patent 876,153, all of whose disclosures areincorporated by reference, the mixture 26 may be prepared with arelatively high content of solvent, so that the volume of theS-EB-S/oil/solvent mixture 26 is large as compared with that of thewater/surfactant mixture 32. The high-shear-rate mixing step 34 producesa dispersion of water/surfactant mixture in S-EB-S/oil/solvent. When,however, the solvent is vacuum stripped and optionally more water isadded in step 36, the relative volume of the remaining (S-EB-S/oil)mixture is much less, so that the dispersion inverts, resulting in the(S-EB-S/oil)-in(water/surfactant) aqueous dispersion of FIG. 2A. Thus,the point in the processing at which the nature of the dispersion is tobe judged is after the stripping step 36, not at earlier stages of theprocess.

Any other operable method for producing a dispersion may be used aswell. Examples of such approaches are disclosed in U.S. Pat. Nos.3,238,173, 3,503,917, and 5,120,765, whose disclosures are incorporatedby reference.

The dispersion prepared by the steps 20-36 is preferably used in a dipforming operation. (Although, as discussed earlier, it may be used inother types of forming and applying techniques as well.) Dip-formingtechnology is generally known for other applications, and will bedescribed only briefly here. A form is provided, numeral 38. Anyoperable form may be used, and examples of such forms of most interestto the inventor include a human hand form 60, FIG. 3, and a cylinderform 62 with a closed end, FIG. 4. The hand form 60 is used to makeelastomeric gloves, and the cylinder form 62 is used to make malecondoms.

Articles are prepared by first dipping the form into a volume of thedispersion, numeral 40, and thereafter evaporating the water (i.e.,drying) and fusing the film, numeral 42. Fusing is typicallyaccomplished by heating the article to a temperature above the softeningpoint of the end blocks of the S-EB-S block copolymer for a period oftime. For conventional S-EB-S block copolymers, the fusing treatment isabout 80-95° C. for a time of about 10-20 minutes in a typical case.However, as discussed herein, the S-EB-S block copolymer may be modifiedto increase their glass transition temperature, so that the fusingtemperature will correspondingly be increased. The times andtemperatures of the fusing treatment may be varied, with shorter timesused for higher temperatures and longer times used for lowertemperatures.

To prepare such an article, a sufficiently large amount of thedispersion is prepared in the manner described and placed into a dippingtank, at ambient temperature. A commercially available form (typicallymade of aluminum, glass, plastic, or porcelain) in the shape of thedesired article is coated with a release agent such as calcium carbonateslurry or calcium stearate. The form is thereafter dipped into the tankand removed slowly, leaving a thin, uniform layer of the aqueousdispersion deposited onto the form, much in the same manner that a layerof paint would be deposited upon the form if it were dipped into acontainer of paint. During dipping, the dispersion is distributed evenlyover the surface of the form by a combination of rotational and wavymotions applied to the form. The form and overlying layer of dispersionare dried in a stream of air to permit the water in the thin elastomericlayer to evaporate, at ambient or elevated temperature. Each dipped anddried layer is typically about 0.03-0.20 millimeters thick. The dippingprocedure is repeated as necessary to build up a layer of the requiredthickness. Thin articles prepared according to the dipping process ofthe invention have thicknesses of from about 0.03 to about 1.0millimeter, depending upon the thickness per layer and the number oflayers. It is difficult to maintain the integrity of layers of less thanabout 0.03 millimeters thickness. It is difficult to prepare articlesmore than about 1.0 millimeter thick by dip forming. After drying andfusion of the film, the article is removed from the form, which is thenreused. The article may be modified or treated in ways consistent withthe present approach as, for example, by powdering the surface to allowit to be slipped onto the body more easily, or provided with acompatible non-powder surface layer to permit easy donning.

The following examples illustrate the application and practice of thepresent invention. These examples are presented by way of illustrationand not of limitation, and should not be interpreted as limiting of theinvention in any respect.

EXAMPLE 1

About 150 grams of a 16 weight percent toluene solution of 40 parts byweight Kraton 1650, 40 parts by weight Kraton 1651, and 10 parts byweight Kraton 1652 S-EB-S block copolymers, and containing 56 phr oil,was dispersed in about 100 grams of water containing 1 gram of EmkolK-8300 surfactant. Dispersion was accomplished with a rotor/statorassembly under high shear conditions for two minutes. The solvent wasstripped off in a rotovap under heat and vacuum, and the solutiondiluted by adding water. The dispersion was used in a dip-formingoperation to form an elastomer film.

EXAMPLE 2

About 150 grams of a cyclohexane solution of 40 parts by weight Kraton1650, 40 parts by weight Kraton 1651, and 10 parts by weight Kraton 1652S-EB-S block copolymers, and containing 48 phr oil, was dispersed inabout 150 grams of water containing 0.67 grams of sulfo-succinatesurfactant. Dispersion was accomplished with a rotor/stator assemblyunder high shear conditions for two minutes. The cyclohexane wasstripped off and the dispersion concentrated to obtain an aqueousdispersion of S-EB-S block copolymer and oil. The dispersion was used ina dip-forming operation to form an elastomer film, which was dried andfused at 80-95° C. for 10-20 minutes. The resulting film exhibitedexcellent mechanical strength properties.

EXAMPLE 3

A dispersion was made as in Example 1, except that the final dispersioncontained 2.5 weight percent Emkol K-8300 surfactant. The film producedin dip forming was fused at 80-95° C. for 10-20 minutes. The resultingfilm exhibited excellent mechanical strength properties.

The present approach provides a technique for forming good-quality filmsfrom an aqueous dispersion. The films have the advantageous propertiesas disclosed in U.S. Pat. Nos. 5,112,900 and 5,407,715, but thedip-forming operation is more economical than the approach described inthese patents. Although a particular embodiment of the invention hasbeen described in detail for purposes of illustration, variousmodifications and enhancements may be made without departing from thespirit and scope of the invention. Accordingly, the invention is not tobe limited except as by the appended claims.

What is claimed is:
 1. A method for the preparation of an elastomericarticle, comprising the steps of:furnishing an aqueous dispersion,comprising:a dispersion medium consisting essentially of a mixture ofwater and a surfactant; and a plurality of particles dispersed in thedispersion medium, each particle comprising a mixture of astyrene-ethylene/butylene-styrene block copolymer, and an oil, whereinthe end blocks of the styrene-ethylene/butylene-styrene block copolymereach have a weight average molecular weight of more than about 15,000Daltons and wherein the end blocks constitute about 25-35 percent byweight of the total molecule; dipping a form into the aqueous dispersionand withdrawing the form from the aqueous dispersion, leaving a film ofthe dispersion on the form; and evaporating the water from thedispersion on the form and heating the resulting film to fuse the film,leaving a coherent extensible film on the form.
 2. The method of claim1, wherein the step of furnishing an aqueous dispersion includes thestep offurnishing a dispersion wherein the particles have an averagesize of no more than about 2 micrometers.
 3. The method of claim 1,wherein the step of furnishing an aqueous dispersion includes the stepoffurnishing a dispersion wherein the styrene-ethylene/butylene-styreneblock copolymer has end blocks each with a weight average molecularweight of more than about 20,000 Daltons.
 4. The method of claim 1,wherein the step of furnishing an aqueous dispersion includes the stepoffurnishing a dispersion wherein the styrene-ethylene/butylene-styreneblock copolymer comprises block copolymers of substantially the samemolecular weight.
 5. The method of claim 1, wherein the step offurnishing an aqueous dispersion includes the step offurnishing adispersion wherein the styrene-ethylene/butylene-styrene block copolymercomprises a mixture of at least two styrene-ethylene/butylene-styreneblock copolymers of different molecular weights.
 6. The method of claim1, wherein the step of furnishing an aqueous dispersion includes thestep offurnishing a dispersion wherein the oil is a mineral oil.
 7. Themethod of claim 1, wherein the step of furnishing an aqueous dispersionincludes the step offurnishing a dispersion wherein the particlescomprise a mixture of from about 30 to about 70 percent by weight oil,balance styrene-ethylene/butylene-styrene block copolymer.
 8. The methodof claim 1, wherein the step of furnishing includes the stepsofpreparing a first mixture comprising styrene-ethylene/butylene-styreneblock copolymer, an oil, and a solvent, preparing a second mixturecomprising water and a surfactant, mixing the first mixture and thesecond mixture together under high-shear conditions to form adispersion, and stripping the solvent from the dispersion.
 9. The methodof claim 1, wherein the step of furnishing includes the stepsofpreparing a first dispersion comprising thestyrene-ethylene/butylene-styrene block copolymer, a solvent and water,stripping the solvent from the first dispersion, preparing a seconddispersion comprising oil and water, and mixing the stripped firstdispersion and the second dispersion together to form a thirddispersion.
 10. An elastomeric article prepared by the method ofclaim
 1. 11. The method of claim 1, wherein the step of furnishing anaqueous dispersion includes the step offurnishing astyrene-ethylene/butylene-styrene copolymer wherein the end blocks ofthe styrene-ethylene/butylene-styrene block copolymer each have a weightaverage molecular weight of from about 20,000 to about 25,000 Daltons.12. The method of claim 1, wherein the step of furnishing an aqueousdispersion includes the step offurnishing astyrene-ethylene/butylene-styrene copolymer having an end blockcompatible resin added to the end styrene blocks.